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Number of items: 67.

Bracher-Smith, Matthew, Rees, Elliott, Menzies, Georgina, Walters, James, O'Donovan, Michael, Owen, Michael J., Kirov, George and Escott-Price, Valentina 2022. Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK Biobank. Schizophrenia Research 246 , pp. 156-164. 10.1016/j.schres.2022.06.006

Wadon, Megan, Fenner, Eilidh, Kendall, Kimberley, Bailey, Grace, Sandor, Cynthia, Rees, Elliott and Peall, Kathryn J. 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 10.1007/s00415-022-11307-4

Clifton, Nicholas, Bosworth, Matthew, Haan, Niels, Rees, Elliott, Holmans, Peter, Wilkinson, Lawrence, Isles, Anthony, Collins, Mark and Hall, Jeremy 2022. Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function. Human Molecular Genetics 10.1093/hmg/ddac105

McAllister, Branduff, Donaldson, Jasmine, Binda, Caroline, Powell, Sophie, Chughtai, Uroosa, Edwards, Gareth, Stone, Joseph, Lobanov, Sergey, Elliston, Linda, Schuhmacher, Laura, Rees, Elliott, Menzies, Georgina, Ciosi, Marc, Maxwell, Alastair, Chao, Michael, Eun Pyo, Hong, Lucente, Diane, Wheeler, Vanessa, Jong-Min, Lee, MacDonald, Marcy, Long, Jeffrey, Aylward, Elizabeth, Landwehrmeyer, G. Bernhard, Rosser, Anne, REGISTRY Investigators of the European Huntington’s disease netw, Paulsen, Jane, PREDICT-HD Investigators of the Huntington Study Group, Williams, Nigel, Gusella, James, Monckton, Darren, Allen, Nicholas, Holmans, Peter, Jones, Lesley and Massey, Thomas 2022. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset. Nature Neuroscience 25 , pp. 446-457. 10.1038/s41593-022-01033-5

Singh, Tarjinder, Schizophrenia Exome Meta-Analysis (SCHEMA) Consortium, Kirov, George, Rees, Elliott, Walters, James, Owen, Michael and O'Donovan, Michael 2022. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 604 , pp. 509-516. 10.1038/s41586-022-04556-w
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Sanders, Bret, D'Andrea, Daniel, Collins, Mark O., Rees, Elliott, Steward, Tom G. J., Zhu, Ying, Chapman, Gareth, Legge, Sophie E., Pardinas, Antonio F., Harwood, Adrian J., Gray, William P., O'Donovan, Michael C., Owen, Michael J., Errington, Adam C., Blake, Derek J., Whitcomb, Daniel J., Pocklington, Andrew J. and Shin, Eunju 2022. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature Communications 13 (1) , 27. 10.1038/s41467-021-27601-0

Creeth, Hugo D. J., Rees, Elliott, Legge, Sophie E., Dennison, Charlotte A., Holmans, Peter, Walters, James T. R., O'Donovan, Michael C. and Owen, Michael J. 2022. Ultra-rare coding variants and cognitive function in schizophrenia. JAMA Psychiatry

Rees, Elliott, Creeth, Hugo, Hwo, Hai-Gwo, Chen, Wei J., Tsuang, Ming, Glatt, Stephen J., Rey, Romain, Kirov, George, Walters, James, Holmans, Peter, Owen, Michael and O'Donovan, Michael 2021. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications 12 , 5353. 10.1038/s41467-021-25532-4

Legge, Sophie, Cardno, Alastair, Allardyce, Judith, Dennison, Charlotte, Hubbard, Leon, Pardinas, Antonio, Richards, Alexander, Rees, Elliott, Di Florio, Arianna, Escott-Price, Valentina, Zammit, Stanley, Holmans, Peter, Owen, Michael J., O'Donovan, Michael C. and Walters, James T. R. 2021. Associations between schizophrenia polygenic liability, symptom dimensions, and cognitive ability in schizophrenia. JAMA Psychiatry 78 (10) , pp. 1143-1151. 10.1001/jamapsychiatry.2021.1961

Clifton, Nicholas E., Rees, Elliott, Holmans, Peter A., Pardinas, Antonio. F., Harwood, Janet, Di Florio, Arianna, Kirov, George, Walters, James T. R., O’Donovan, Michael C., Owen, Michael J., Hall, Jeremy and Pocklington, Andrew J. 2021. Genetic association of FMRP targets with psychiatric disorders. Molecular Psychiatry 26 , pp. 2977-2990. 10.1038/s41380-020-00912-2

Hubbard, Leon, Rees, Elliott, Morris, Derek W., Lynham, Amy J., Richards, Alex L., Pardinas, Antonio F., Legge, Sophie E., Harold, Denise, Zammit, Stanley, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Donohoe, Gary, Kirov, George, Pocklington, Andrew and Walters, James T.R. 2021. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 90 (1) , pp. 28-34. 10.1016/j.biopsych.2020.11.025

Rees, Elliott and Kirov, George 2021. Copy number variation and neuropsychiatric illness. Current Opinion in Genetics and Development 68 , pp. 57-63. 10.1016/j.gde.2021.02.014

Caseras, Xavier, Kirov, George, Kendall, Kimberley M., Rees, Elliott, Legge, Sophie E., Bracher-Smith, Matthew, Escott-Price, Valentina and Murphy, Kevin 2021. Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank. British Journal of Psychiatry 218 (2) , pp. 104-111. 10.1192/bjp.2020.139

Kendall, Kimberley M., John, Ann, Lee, Sze Chim, Rees, Elliott, Pardiñas, Antonio F., Del Pozo Banos, Marcos, Owen, Michael J., O’Donovan, Michael C., Kirov, George, Lloyd, Keith, Jones, Ian, Legge, Sophie E. and Walters, James T. R. 2020. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: a data linkage study. BJPsych Open 6 (6) , e139. 10.1192/bjo.2020.42

Legge, Sophie, Dennison, Charlotte, Pardinas, Antonio, Rees, Elliott, Lynham, Amy, Hopkins, Lucinda, Bates, Lesley, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2020. Clinical indicators of treatment-resistant psychosis. British Journal of Psychiatry 216 (5) , pp. 259-266. 10.1192/bjp.2019.120

Martin, Joanna, Hosking, Grace, Wadon, Megan, Agha, Sharifah Shameem, Langley, Kate, Rees, Elliott, Owen, Michael, O'Donovan, Michael, Kirov, George and Thapar, Anita 2020. A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. Translational Psychiatry 10 , 135. 10.1038/s41398-020-0821-y

Warland, Anthony, Kendall, Kimberley M., Rees, Elliott, Kirov, George and Caseras, Xavier 2020. Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank. Molecular Psychiatry 25 (4) , pp. 854-862. 10.1038/s41380-019-0355-y

Rees, Elliott and Owen, Michael J. 2020. Translating insights from neuropsychiatric genetics and genomics for precision psychiatry. Genome Medicine 12 (1) , 43. 10.1186/s13073-020-00734-5

Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott, Bergen, Sarah, Hultman, Christina, Kirov, George, O'Donovan, Michael, Owen, Michael, Holmans, Peter, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J. and Ruderfer, Douglas M. 2020. Characterization of single gene copy number variants in schizophrenia. Biological Psychiatry 87 (8) , pp. 736-744. 10.1016/j.biopsych.2019.09.023

Rees, Elliott, GROUP Investigators, Han, Jun, Morgan, Joanne, Carrera, Noa, Escott-Price, Valentina, Pocklington, Andrew J., Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardinas, Antonio F., Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George, Walters, James T. R., Holmans, Peter, O'Donovan, Michael C. and Owen, Michael J. 2020. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience 23 (2) , pp. 179-184. 10.1038/s41593-019-0565-2

Hall, Lynsey S, Medway, Christopher W, Pain, Oliver, Pardinas, Antonio F, Rees, Elliott G, Escott-Price, Valentina, Pocklington, Andrew, Bray, Nicholas J, Holmans, Peter A, Walters, James T R, Owen, Michael and O'Donovan, Michael 2020. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics 29 (1) , pp. 159-167. 10.1093/hmg/ddz253

Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M., Pardinas, Antonio F., Menzies, Georgina, Bracher-Smith, Matthew, Escott-Price, Valentina, Rees, Elliott, Davis, Katrina A., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter, Kirov, George, Owen, Michael J., O'Donovan, Michael C., Zammit, Stanley and Walters, James T. R. 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12) , pp. 1256-1265. 10.1001/jamapsychiatry.2019.2508

Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J, Forrest, Marc P, Tansey, Katherine E, Pardinas, Antonio F., Rees, Elliott, Doyle, A. Michelle, Wilkinson, Lawrence S., Owen, Michael J., O'Donovan, Michael and Blake, Derek J. 2019. Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression. Schizophrenia Bulletin 45 (6) , pp. 1267-1278. 10.1093/schbul/sby183

Kendall, Kimberley M., Bracher-Smith, Matthew, Fitzpatrick, Harry, Lynham, Amy, Rees, Elliott, Escott-Price, Valentina, Owen, Michael J., O'Donovan, Michael C., Walters, James T.R. and Kirov, George 2019. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. British Journal of Psychiatry 214 (05) , pp. 297-304. 10.1192/bjp.2018.301

Kendall, Kimberley M, Rees, Elliott, Bracher-Smith, Matthew, Legge, Sophie, Riglin, Lucy, Zammit, Stanley, O'Donovan, Michael Conlon, Owen, Michael John, Jones, Ian, Kirov, George and Walters, James Tynan Rhys 2019. Association of rare copy number variants with risk of depression. JAMA Psychiatry 76 (8) , pp. 818-825. 10.1001/jamapsychiatry.2019.0566

Rees, Elliott, Carrera, Noa, Morgan, Joanne, Hambridge, Kirsty, Escott-Price, Valentina, Pocklington, Andrew J., Richards, Alexander L., Pardinas, Antonio F., McDonald, Colm, Donohoe, Gary, Morris, Derek W., Kenny, Elaine, Kelleher, Eric, Gill, Michael, Corvin, Aiden, Kirov, George, Walters, James T. R., Holmans, Peter, Owen, Michael J. and O'Donovan, Michael C. 2019. Targeted sequencing of 10,198 samples confirms abnormalities in neuronal activity and implicates voltage-gated sodium channels in schizophrenia pathogenesis. Biological Psychiatry 85 (7) , pp. 554-562. 10.1016/j.biopsych.2018.08.022

Vadgama, Nirmal, Pittman, Alan, Simpson, Michael, Nirmalananthan, Niranjanan, Murray, Robin, Yoshikawa, Takeo, De Rijk, Peter, Rees, Elliott, Kirov, George, Hughes, Deborah, Fitzgerald, Tomas, Kristiansen, Mark, Pearce, Kerra, Cerveira, Eliza, Zhu, Qihui, Zhang, Chengsheng, Lee, Charles, Hardy, John and Nasir, Jamal 2019. De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes. European Journal of Human Genetics 27 (7) , pp. 1121-1133. 10.1038/s41431-019-0376-7

Drakesmith, Mark, Parker, Greg D., Smith, Jacqueline, Linden, Stefanie C., Rees, Elliott, Williams, Nigel, Owen, Michael J., van den Bree, Marianne, Hall, Jeremy, Jones, Derek K. and Linden, David E. J. 2019. Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures. Translational Psychiatry 9 (1) , 102. 10.1038/s41398-019-0440-7

Crawford, Karen, Bracher-Smith, Matthew, Owen, David, Kendall, Kimberley M., Rees, Elliott, Pardinas, Antonio F., Einon, Mark, Escott-Price, Valentina, Walters, James T. R., O'Donovan, Michael C., Owen, Michael J. and Kirov, George 2019. Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank. Journal of Medical Genetics 56 , pp. 131-138. 10.1136/jmedgenet-2018-105477

Owen, David, Bracher Smith, Mathew, Kendall, Kimberley M., Rees, Elliott, Einon, Mark, Escott-Price, Valentina, Owen, Michael J., O'Donovan, Michael C. and Kirov, George 2018. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank. BMC Genomics 19 (1) , 867. 10.1186/s12864-018-5292-7

Pardinas, Antonio F., GERAD Consortium, Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda, Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nichols G., McIntosh, Andrew M., Plomin, Robert P., Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Eeben A., Als, Thomas P., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bocker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Giørtz Pedersenu, Marianne, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Søholm Hansen, Christine, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J, O'Donovan, Michael C., Walters, James T. R., Williams, Julie and CRESTAR Consortium 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics 50 , pp. 381-389. 10.1038/s41588-018-0059-2

Legge, S. E., Hamshere, M. L., Ripke, S., Pardinas, A. F., Goldstein, J. I., Rees, E., Richards, A. L., Leonenko, G., Jorskog, L. F., Goldstein, J. I., Jarskog, L. F., Hilliard, C., Alfirevic, A., Duncan, L., Fourches, D., Huang, H., Lek, M., Neale, B. M., Ripke, S., Shianna, K., Szatkiewicz, J. P., Tropsha, A., van den Oord, E. J. C. G., Cascorbi, I., Dettling, M., Gazit, E., Goff, D. C., Holden, A. L., Kelly, D. L., Malhotra, A. K, Nielsen, J., Pirmohamed, M., Rujescu, D., Werge, T., Levy, D. L., Josiassen, R. C., Kennedy, J. L., Lieberman, J. A., Daly, M. J., Sullivan, P. F., Chambert, K. D., Collier, D. A., Genovese, G., Giegling, I., Holmans, P., Jonasdottir, A., Kirov, G., McCarroll, S. A., MacCabe, J. H., Mantripragada, K, Moran, J. L., Neale, B. M., Stefansson, H., Rujescu, D., Daly, M. J., Sullivan, P. F., Owen, M. J., O'Donovan, M. C. and Walters, J.T. R 2017. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry 22 , pp. 1502-1508. 10.1038/mp.2016.97

Singh, Tarjinder, Walters, James T. R., Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M., Kirov, George, Geschwind, Daniel, Murray, Robin M, Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M., Sklar, Pamela, Palotie, Aarno, Sullivan, Patrick F., O'Donovan, Michael C., Owen, Michael J. and Barrett, Jeffrey C. 2017. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nature Genetics 49 , pp. 1167-1173. 10.1038/ng.3903

Kendall, Kimberley M., Rees, Elliott, Escott-Price, Valentina, Einon, Mark, Thomas, Rhys, Hewitt, Jonathan, O'Donovan, Michael C., Owen, Michael J., Walters, James T. R. and Kirov, George 2017. Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK Biobank subjects. Biological Psychiatry 82 (2) , P103-110. 10.1016/j.biopsych.2016.08.014

Huang, Alden Y., Yu, Dongmei, Davis, Lea K., Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A., McGrath, Lauren M., Illmann, Cornelia, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Dion, Yves, Rouleau, Guy, Budman, Cathy L., Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R., Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J., McMahon, William M., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R., Rizzo, Renata, Cath, Danielle C., Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A., Okun, Michael S., Woods, Douglas W., Rees, Elliott, Pato, Carlos N., Pato, Michele T., Knowles, James A., Posthuma, Danielle, Pauls, David L., Cox, Nancy J., Neale, Benjamin M., Freimer, Nelson B., Paschou, Peristera, Mathews, Carol A., Scharf, Jeremiah M. and Coppola, Giovanni 2017. Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette Syndrome. Neuron 94 (6) , 1101-1111.e7. 10.1016/j.neuron.2017.06.010

Clifton, N. E., Pocklington, A. J., Scholz, B., Rees, E., Walters, J. T. R., Kirov, G., O'Donovan, M. C., Owen, M. J., Wilkinson, L. S., Thomas, K. L. and Hall, J. 2017. Schizophrenia copy number variants and associative learning. Molecular Psychiatry 22 (2) , pp. 178-182. 10.1038/mp.2016.227

Rees, Elliott, Kendall, Kimberley, Pardinas, Antonio F., Legge, Sophie E., Pocklington, Andrew, Escott-Price, Valentina, MacCabe, James H., Collier, David A., Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Walters, James T. R. and Kirov, George 2016. Analysis of intellectual disability copy number variants for association with schizophrenia. JAMA Psychiatry 73 (9) , pp. 963-969. 10.1001/jamapsychiatry.2016.1831

Tansey, K. E., Rees, E., Linden, D. E., Ripke, S., Chambert, D., Moran, J. L., McCarroll, S. A., Holmans, P., Kirov, G., Walters, J., Owen, M. J. and O'Donovan, M. C. 2016. Common alleles contribute to schizophrenia in CNV carriers. Molecular Psychiatry 21 , pp. 1085-1089. 10.1038/mp.2015.143

Pardinas, Antonio, Holmans, Peter, Pocklington, Andrew, Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Stephen A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Consortium, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. [Online]. bioRxiv. Available at: http://dx.doi.org/10.1101/068593

Han, Jun, Walters, James, Kirov, George, Pocklington, Andrew, Escott-Price, Valentina, Owen, Michael John, Holmans, Peter Alan, O'Donovan, Michael Conlon and Rees, Elliott 2016. Gender differences in CNV burden do not confound schizophrenia CNV associations. Scientific Reports 6 , 25986. 10.1038/srep25986

Isles, Anthony R., Ingason, Andrés, Lowther, Chelsea, Walters, James, Gawlick, Micha, Stöber, Gerald, Rees, Elliott, Martin, Joanna, Little, Rosie B., Potter, Harry, Georgieva, Lyudmila, Pizzo, Lucilla, Ozaki, Norio, Aleksic, Branko, Kushima, Itaru, Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Shi, Jianxin, Sanders, Alan R., Duan, Jubao, Willis, Joseph, Sisodiya, Sanjay, Costain, Gregory, Werge, Thomas M., Degenhardt, Franziska, Giegling, Ina, Rujescu, Dan, Hreidarsson, Stefan J., Saemundsen, Evald, Ahn, Joo Wook, Ogilvie, Caroline, Girirajan, Santhosh D., Stefansson, Hreinn, Stefansson, Kari, O'Donovan, Michael C., Owen, Michael J., Bassett, Anne and Kirov, George 2016. Parental origin of interstitial duplications at 15q11.2-q13.3 in schizophrenia and neurodevelopmental disorders. PLoS Genetics 12 (5) , e1005993. 10.1371/journal.pgen.1005993

Singh, Tarjinder, Swedish Schizophrenia Study, Kurki, Mitja I, Curtis, David, Purcell, Shaun M, Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietiläinen, Olli, Gerety, Sebastian S., Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L, Craddock, Nick, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B., Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, George, Körkkö, Jarmo, Kuismin, Outi, Holmans, Peter, Hultman, Christina M., Iyegbe, Conrad, Lönnqvist, Jouko, Männikkö, Minna, McCarroll, Steve A., McGuffin, Peter, McIntosh, Andrew M., McQuillin, Andrew, Moilanen, Jukka S., Moore, Carmel, Murray, Robin M., Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, Clair, David St, Veijola, Juha, Walters, James T. R., Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E., O'Donovan, Michael C., Palotie, Aarno, Owen, Michael J., Barrett, Jeffrey C., INTERVAL Study, DDD Study and UK10 K Consortium 2016. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nature Neuroscience 19 (4) , pp. 571-577. 10.1038/nn.4267

Fry, Andrew Evan, Rees, Elliott, Thompson, Rose, Mantripragada, Kiran, Blake, Penny, Jones, Glyn, Morgan, Sian, Jose, Sian, Mugalaasi, Hood, Archer, Hayley, McCann, Emma, Clarke, Angus John, Taylor, Clare, Davies, Sally, Gibbon, Frances, Te Water Naude, Johann, Hartley, Louise, Thomas, Gareth, White, Catharine, Natarajan, Jaya, Thomas, Rhys H., Drew, Cheney, Chung, Seo-Kyung, Rees, Mark I., Holmans, Peter Alan, Owen, Michael John, Kirov, George, Pilz, Daniela T. and Kerr, Michael Patrick 2016. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC Medical Genetics 17 , -. 10.1186/s12881-016-0294-2

Singh, Tarjinder, Kurki, Mitja I., Curtis, David, Purcell, Shaun M., Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietilainen, Olli, Gerety, Sebastian S., Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L., Craddock, Nicholas John, Daly, Mark J., Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B., Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, George, Korkko, Jarmo, Kuismin, Outi, Holmans, Peter Alan, Hultman, Christina M., Iyegbe, Conrad, Lonnqvist, Jouko, Mannikko, Minna, McCaroll, Steve A., McGuffin, Peter, McIntosh, Andrew M., McQuillin, Andrew, Moilanen, Jukka S., Moore, Carmel, Murray, Robin M., Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, St Clair, David, Vejola, Juha, Walters, James Tynan Rhys, Williams, Hywel, Swedish Schizophrenia Study, INTERVAL Study, DDD Study, UKK Consortium, Sullivan, Patrick F., Hurles, Matthew E., O'Donovan, Michael Conlon, Palotie, Aarno, Owen, Michael John and Barrett, Jeffrey C. 2016. Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders. Nature Neuroscience 19 , pp. 571-577. 10.1101/036384

Richards, Alexander, Leonenko, Ganna M, Walters, James Tynan Rhys, Kavanagh, D, Rees, Elliott, Evans, Anna, Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, Andrew, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2016. Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics 25 (5) , pp. 1001-1007. 10.1093/hmg/ddv620

Tansey, Katherine E., Rees, Elliott, Linden, David Edmun Johannes, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, Peter Alan, Kirov, George, Walters, James Tynan Rhys, Owen, Michael John and O'Donovan, Michael Conlon 2015. Common alleles contribute to schizophrenia in CNV carriers [Erratum]. Molecular Psychiatry 21 , 1153. 10.1038/mp.2015.170

Escott-Price, Valentina, Kirov, George, Rees, Elliott, Isles, Anthony Roger, Owen, Michael John and O'Donovan, Michael Conlon 2015. No evidence for enrichment in schizophrenia for common allelic associations at imprinted loci. PLoS ONE 10 (12) , -. 10.1371/journal.pone.0144172

Heyes, Samuel, Pratt, Wendy S., Rees, Elliott, Dahimene, Shehrazade, Ferron, Laurent, Owen, Michael John and Dolphin, Annette C. 2015. Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology 134 , pp. 36-54. 10.1016/j.pneurobio.2015.09.002

Pocklington, Andrew, Rees, Elliott, Walters, James T. R., Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter, Moran, Jennifer L., McCarroll, Steven A., Kirov, George, O'Donovan, Michael C. and Owen, Michael J. 2015. Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia. Neuron 86 (5) , pp. 1203-1214. 10.1016/j.neuron.2015.04.022

Kirov, George, Rees, Elliott and Walters, James Tynan Rhys 2015. What a psychiatrist needs to know about copy number variants. BJPscyh Advances 21 (3) , pp. 157-163. 10.1192/apt.bp.113.012039

Rees, Elliott, O'Donovan, Michael Conlon and Owen, Michael John 2015. Genetics of schizophrenia. Current Opinion in Behavioral Sciences 2 , pp. 8-14. 10.1016/j.cobeha.2014.07.001

Green, E. K., Rees, E., Walters, J. T. R., Smith, K-G, Forty, L., Grozeva, D., Moran, J. L., Sklar, P., Ripke, S., Chambert, K. D., Genovese, G., McCarroll, S. A., Jones, I., Jones, L., Owen, M. J., O'Donovan, M. C., Craddock, N. and Kirov, G. 2015. Copy number variation in bipolar disorder. Molecular Psychiatry 21 (1) , pp. 89-93. 10.1038/mp.2014.174

Rees, Elliott, Kirov, George, Walters, James Tynan Rhys, Richards, Alexander, Howrigan, D., Kavanagh, D. H., Pocklington, Andrew, Fromer, M., Ruderfer, D..M., Georgieva, Lyudmila, Carrera, Noa, Gormley, P., Palta, P., Williams, H., Dwyer, S., Johnson, J. S., Roussos, P., Barker, D. D., Banks, E., Milanova, V., Rose, S .A., Chambert, K., Mahajan, M, Scolnick, E. M., Moran, J. L., Tsuang, M. T., Glatt, S. J., Chen, W. J., Hwu, H.-G., Faraone, Stephen V., Roe, Cheri A., Chandler, Sharon D., Liu, Chih-Min, Liu, Chen-Chung, Yeh, Ling-Ling, Ouyang, Wen-Chen, Chan, Hung-Yu, Chen, Chun-Ying, Neale, B. M., Palotie, A., Sklar, P., Purcell, S. M., McCarroll, S .A., Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2015. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry 5 (7) , e607. 10.1038/tp.2015.99

Georgieva, Lyudmila, Rees, Elliott, Moran, Jennifer L., Chambert, Kimberly D., Milanova, Vihra, Craddock, Nicholas, Purcell, Shaun, Sklar, Pamela, McCarroll, Steven, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J. and Kirov, George 2014. De novo CNVs in bipolar affective disorder and schizophrenia. Human Molecular Genetics 23 (24) , pp. 6677-6683. 10.1093/hmg/ddu379

Szatkiewicz, J. P., O'Dushlaine, C., Chen, G., Chambert, K., Moran, J. L., Neale, B. M., Fromer, M., Ruderfer, D., Akterin, S., Bergen, S. E., Kähler, A., Magnusson, P. K. E., Kim, Y., Crowley, J..J., Rees, E., Kirov, G., O'Donovan, M. C., Owen, M. J., Walters, J. T. R., Scolnick, E., Sklar, P., Purcell, S., Hultman, C. M., McCarroll, S. A. and Sullivan, P. F. 2014. Copy number variation in schizophrenia in Sweden. Molecular Psychiatry 19 (7) , pp. 762-773. 10.1038/mp.2014.40

Rees, Elliott, Walters, James Tynan Rhys, Owen, Michael John and Kirov, George 2014. Authors' reply [Letter]. British Journal of Psychiatry 205 (1) , p. 78. 10.1192/bjp.205.1.78

Morris, D. W., Pearson, R. D., Cormican, P., Kenny, E. M., O'Dushlaine, C. T., Perreault, L.-P. L., Giannoulatou, E., Tropea, D., Maher, B. S., Wormley, B., Kelleher, E., Fahey, C., Molinos, I., Bellini, S., Pirinen, M., Strange, A., Freeman, C., Thiselton, D. L., Elves, R. L., Regan, R., Ennis, S., Dinan, T. G., McDonald, C., Murphy, K. C., O'Callaghan, E., Waddington, J. L., Walsh, D., O'Donovan, Michael Conlon, Grozeva, Detelina, Craddock, Nicholas John, Stone, J., Scolnick, E., Purcell, S., Sklar, P., Coe, B., Eichler, E. E., Ophoff, R., Buizer, J., Szatkiewicz, J., Hultman, C., Sullivan, P., Gurling, H., Mcquillin, A., St Clair, D., Rees, Elliott, Kirov, George, Walters, James Tynan Rhys, Blackwood, D., Johnstone, M., Donohoe, G., O'Neill, F. A., Kendler, K. S., Gill, M., Riley, B. P., Spencer, C. C. A. and Corvin, A. 2014. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics 23 (12) , pp. 3316-3326. 10.1093/hmg/ddu025

Rees, Elliott, Walters, James t. R., Chambert, Kimberley D., O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L., Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., Genovese, Guilio, Levinson, Douglas, Morris, Derek W., Cormican, Paul, Kendler, Kenneth S., O'Neill, Francis A., Riley, Brian, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina H., Pato, Carlos, Pato, Michelle, Sullivan, Patrick F., Gejman, Pablo V., McCarroll, Stephen A., O'Donovan, Michael C., Owen, Michael J. and Kirov, George 2014. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics 23 (6) , pp. 1669-1676. 10.1093/hmg/ddt540

Rees, Elliott, Walters, James T. R., Georgieva, Lyudmila, Isles, Anthony R., Chambert, Kimberley D., Richards, Alexander L., Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Stephen A., O'Donovan, Michael C., Owen, Michael J. and Kirov, George 2014. Analysis of copy number variations at 15 schizophrenia-associated loci. British Journal of Psychiatry 204 (2) , pp. 108-114. 10.1192/bjp.bp.113.131052

Fromer, Menachem, Pocklington, Andrew, Kavanagh, David, Williams, Hywel J., Dwyer, Sarah, Gormley, Padhraig, Georgieva, Lyudmila, Rees, Elliott, Palta, Priit, Ruderfer, Douglas, Carrera, Noa, Humphreys, Isla, Johnson, Jessica S., Roussos, Panos, Barker, Douglas D., Banks, Eric, Milanova, Vihra, Grant, Seth G., Hannon, Eilis, Rose, Samuel A., Chambert, Kimberly, Mahajan, Milind, Scolnick, Edward M., Moran, Jennifer L., Kirov, George, Palotie, Aarno, McCarroll, Steven A., Holmans, Peter, Sklar, Pamela, Owen, Michael J., Purcell, Shaun M. and O'Donovan, Michael C. 2014. De novo mutations in schizophrenia implicate synaptic networks. Nature 506 , pp. 179-184. 10.1038/nature12929

Rees, Elliott, Kirov, George, Sanders, A., Walters, James Tynan Rhys, Chambert, K. D., Shi, J., Szatkiewicz, J., O'Dushlaine, C., Richards, Alexander L., Green, Elaine Karen, Jones, Ian Richard, Davies, Geraint, Legge, Sophie E., Moran, J. L., Pato, C., Pato, M., Genovese, G., Levinson, D., Duan, J., Moy, W., Göring, H. H. H., Morris, D., Cormican, P., Kendler, K. S., O'Neill, F. A., Riley, B., Gill, M., Corvin, A., Craddock, Nicholas John, Sklar, P., Hultman, C., Sullivan, P. F., Gejman, P. V., McCarroll, S. A., O'Donovan, Michael Conlon and Owen, Michael John 2013. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry n/a 10.1038/mp.2013.156

Guha, Saurav, Rees, Elliott, Darvasi, Ariel, Ivanov, Dobril, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K., Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M., Moran, Jennifer L., Chambert, Kimberly D., Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill,, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M., Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael John, O'Donovan, Michael Conlon, Lencz, Todd and Kirov, George 2013. Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 70 (3) , pp. 253-260. 10.1001/2013.jamapsychiatry.71

Chapman, J., Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, P, Stretton, A., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon, Williams, Julie and Kirov, George 2013. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics 22 (4) , pp. 816-824. 10.1093/hmg/dds476

Kirov, George, Rees, Elliott, Walters, James Tynan Rhys, Escott-Price, Valentina, Georgieva, Lyudmila, Richards, Alexander, Chambert, Kimberly D., Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O'Donovan, Michael Conlon and Owen, Michael John 2013. The penetrance of copy number variations for schizophrenia and developmental delay. Biological Psychiatry 75 (5) , pp. 378-385. 10.1016/j.biopsych.2013.07.022

Rees, Elliott, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2012. De Novo mutation in schizophrenia. Schizophrenia Bulletin 38 (3) , pp. 377-381. 10.1093/schbul/sbs047

Kirov, George, Pocklington, Andrew, Holmans, Peter Alan, Ivanov, Dobril, Ikeda, M., Ruderfer, D., Moran, J., Chambert, K., Toncheva, D., Georgieva, Lyudmila, Grozeva, Detelina, Fjodorova, Marija, Wollerton, Rebecca Louise, Rees, Elliott, Nikolov, Ivan, van de Lagemaat, L. N., Bayés, À., Fernandez, E., Olason, P. I., Böttcher, Y., Komiyama, N. H., Collins, M. O., Choudhary, J., Stefansson, K., Stefansson, H., Grant, S. G. N., Purcell, S., Sklar, P., O'Donovan, Michael Conlon and Owen, Michael John 2012. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular Psychiatry 17 (2) , pp. 142-153. 10.1038/mp.2011.154

Rees, Elliott, Escott-Price, Valentina, Owen, Michael John, O'Donovan, Michael Conlon and Kirov, George 2011. De novo rates and selection of schizophrenia-associated copy number variants. Biological Psychiatry 70 (12) , pp. 1109-1114. 10.1016/j.biopsych.2011.07.011

This list was generated on Sun Aug 7 04:04:26 2022 BST.